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The Mitochondrial ATPase Inhibitory Factor 1 Triggers a ROS-Mediated Retrograde Prosurvival and Proliferative Response

AutorFormentini, Laura ; Sánchez-Aragó, María ; Sánchez-Cenizo, Laura ; Cuezva, José M.
Fecha de publicación30-mar-2012
EditorCell Press
CitaciónMolecular Cell 45: 731- 742 (2012)
ResumenRecent findings indicate that prevalent human carcinomas overexpress the mitochondrial ATPase Inhibitory Factor 1 (IF1). Overexpression of IF1 inhibits the synthase activity of the mitochondrial H +-ATP synthase and plays a crucial role in metabolic adaptation of cancer cells to enhanced aerobic glycolysis. Herein, we demonstrate that IF1 overexpression in colon cancer cells triggers mitochondrial hyperpolarization and the subsequent production of superoxide radical, a reactive oxygen species (ROS). ROS are required to promote the transcriptional activation of the NFκB pathway via phosphorylation-dependent IκBα degradation. Activation of NFκB results in a cellular adaptive response that includes proliferation and Bcl-xL mediated resistance to drug-induced cell death. Quenching the mitochondrial production of ROS prevents the activation of NFκB and abolishes the IF1-mediated cellular adaptive response. Overall, our findings provide evidence linking the activity of a mitochondrial protein with retrograde signaling to the nucleus to promote cellular proliferation and survival.
URIhttp://hdl.handle.net/10261/114818
DOI10.1016/j.molcel.2012.01.008
Identificadoresdoi: 10.1016/j.molcel.2012.01.008
issn: 1097-2765
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